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PCCB c.967-6796C>T
Variant ID: 3-136028987-C-T
NM_000532.4(
PCCB
):c.967-6796C>T
This variant was identified in 1 publication
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Genetics-informed precision treatment formulation in schizophrenia and bipolar disorder.
American Journal Of Human Genetics
Reay, William R WR; Geaghan, Michael P MP; Atkins, Joshua R JR; Carr, Vaughan J VJ; Green, Melissa J MJ; Cairns, Murray J MJ
Publication Date: 2022-09-01
Variant appearance in text: rs480330
PubMed Link:
36055211
Variant Present in the following documents:
mmc1.pdf
mmc4.pdf
View BVdb publication page